US8536182B2 - Benzylpiperazine derivatives and their medical use - Google Patents
Benzylpiperazine derivatives and their medical use Download PDFInfo
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- US8536182B2 US8536182B2 US11/996,650 US99665006A US8536182B2 US 8536182 B2 US8536182 B2 US 8536182B2 US 99665006 A US99665006 A US 99665006A US 8536182 B2 US8536182 B2 US 8536182B2
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- phenyl
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- 0 *.[1*]C1CC([2*])CN(CC)C1.[3*][Y]C1CCN(C(=O)CC)CC1 Chemical compound *.[1*]C1CC([2*])CN(CC)C1.[3*][Y]C1CCN(C(=O)CC)CC1 0.000 description 33
- OKLSPPNBXPEEJR-UHFFFAOYSA-N CC(C)NC1=CC=CC(F)=C1 Chemical compound CC(C)NC1=CC=CC(F)=C1 OKLSPPNBXPEEJR-UHFFFAOYSA-N 0.000 description 5
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- FZLHANNVIOUDNV-UHFFFAOYSA-N CC(C)C(=O)OP Chemical compound CC(C)C(=O)OP FZLHANNVIOUDNV-UHFFFAOYSA-N 0.000 description 1
- FCJVIALJMINVOV-UHFFFAOYSA-N CC(C)NC1=CC=C(C(F)(F)F)C=C1 Chemical compound CC(C)NC1=CC=C(C(F)(F)F)C=C1 FCJVIALJMINVOV-UHFFFAOYSA-N 0.000 description 1
- RMXBOQCXULAXBO-UHFFFAOYSA-N CC(C)NC1=CC=C(F)C=C1 Chemical compound CC(C)NC1=CC=C(F)C=C1 RMXBOQCXULAXBO-UHFFFAOYSA-N 0.000 description 1
- OJZKKEGJFOAAAV-UHFFFAOYSA-N CC(C)OC1=CC=C(C#N)C=C1 Chemical compound CC(C)OC1=CC=C(C#N)C=C1 OJZKKEGJFOAAAV-UHFFFAOYSA-N 0.000 description 1
- RGSXYZQTHPVPAF-UHFFFAOYSA-N CC1=CC(C(C(=O)OP)C(=O)OP)=CC=C1C1OCCO1 Chemical compound CC1=CC(C(C(=O)OP)C(=O)OP)=CC=C1C1OCCO1 RGSXYZQTHPVPAF-UHFFFAOYSA-N 0.000 description 1
- DJXCRKJZMOUEPY-JOCHJYFZSA-N CC1=CC=CC(NC2CCN(C(=O)CC3=CC=C(CN4CCC[C@@H](C)C4)C=C3)CC2)=C1 Chemical compound CC1=CC=CC(NC2CCN(C(=O)CC3=CC=C(CN4CCC[C@@H](C)C4)C=C3)CC2)=C1 DJXCRKJZMOUEPY-JOCHJYFZSA-N 0.000 description 1
- SRDGIIKXORBGMO-HXUWFJFHSA-N COC1=C(CN2CCC[C@@H](C)C2)C=CC(CC(=O)N2CCC(NC3=CC(F)=CC=C3)CC2)=C1 Chemical compound COC1=C(CN2CCC[C@@H](C)C2)C=CC(CC(=O)N2CCC(NC3=CC(F)=CC=C3)CC2)=C1 SRDGIIKXORBGMO-HXUWFJFHSA-N 0.000 description 1
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- VIPWUFMFHBIKQI-UHFFFAOYSA-N COc(cc1)ccc1F Chemical compound COc(cc1)ccc1F VIPWUFMFHBIKQI-UHFFFAOYSA-N 0.000 description 1
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- XMXGARVYQJOCFS-HXUWFJFHSA-N C[C@@H]1CCCN(CC2=CC=C(CC(=O)N3CCC(NC4=CC(C#N)=C(F)C=C4)CC3)C=C2)C1 Chemical compound C[C@@H]1CCCN(CC2=CC=C(CC(=O)N3CCC(NC4=CC(C#N)=C(F)C=C4)CC3)C=C2)C1 XMXGARVYQJOCFS-HXUWFJFHSA-N 0.000 description 1
- TUEYZBHUPRMPLA-JOCHJYFZSA-N C[C@@H]1CCCN(CC2=CC=C(CCC(=O)N3CCC(CC4=CC=C(F)C=C4)CC3)C=C2)C1 Chemical compound C[C@@H]1CCCN(CC2=CC=C(CCC(=O)N3CCC(CC4=CC=C(F)C=C4)CC3)C=C2)C1 TUEYZBHUPRMPLA-JOCHJYFZSA-N 0.000 description 1
- BTBRRSURJMDSIM-OAQYLSRUSA-N C[C@@H]1CCCN(CC2=CC=C(CCC(=O)N3CCC(CC4=CC=CC(F)=C4)CC3)N=C2)C1 Chemical compound C[C@@H]1CCCN(CC2=CC=C(CCC(=O)N3CCC(CC4=CC=CC(F)=C4)CC3)N=C2)C1 BTBRRSURJMDSIM-OAQYLSRUSA-N 0.000 description 1
- HOTLFLYDODUURG-SFHVURJKSA-N C[C@@H]1NCCN(Cc2ccc(CC(N(CC3)CCC3Nc3cccc(F)c3)=O)cc2Cl)C1 Chemical compound C[C@@H]1NCCN(Cc2ccc(CC(N(CC3)CCC3Nc3cccc(F)c3)=O)cc2Cl)C1 HOTLFLYDODUURG-SFHVURJKSA-N 0.000 description 1
- KHIMHWLYCZNAGK-FQEVSTJZSA-N C[C@H]1CCCN(CC2=CC=C(CC(=O)N3CCC(NC4=CC(F)=CC=C4)CC3)C=C2)C1 Chemical compound C[C@H]1CCCN(CC2=CC=C(CC(=O)N3CCC(NC4=CC(F)=CC=C4)CC3)C=C2)C1 KHIMHWLYCZNAGK-FQEVSTJZSA-N 0.000 description 1
- RRUNITTWZGAOMK-SZPZYZBQSA-N C[C@H]1C[C@@H](C)CN(CC2=CC=C(C(C)(C)C(=O)N3CCC(NC4=CC=C(F)C=C4)CC3)C=C2)C1 Chemical compound C[C@H]1C[C@@H](C)CN(CC2=CC=C(C(C)(C)C(=O)N3CCC(NC4=CC=C(F)C=C4)CC3)C=C2)C1 RRUNITTWZGAOMK-SZPZYZBQSA-N 0.000 description 1
- MHKDECGGLCCIRR-OYRHEFFESA-N C[C@H]1C[C@@H](C)CN(CC2=CC=C(CC(=O)N3CCC(NC4=CC=C(F)C=C4)CC3)C=C2)C1 Chemical compound C[C@H]1C[C@@H](C)CN(CC2=CC=C(CC(=O)N3CCC(NC4=CC=C(F)C=C4)CC3)C=C2)C1 MHKDECGGLCCIRR-OYRHEFFESA-N 0.000 description 1
- YHFXTGFKYAXQKV-ZRZAMGCNSA-N C[C@H]1C[C@@H](C)CN(CC2=CC=C(CCC(=O)N3CCC(CC4=CC=C(F)C=C4)CC3)C=C2)C1 Chemical compound C[C@H]1C[C@@H](C)CN(CC2=CC=C(CCC(=O)N3CCC(CC4=CC=C(F)C=C4)CC3)C=C2)C1 YHFXTGFKYAXQKV-ZRZAMGCNSA-N 0.000 description 1
- UDEXLEROVMQATR-ONEGZZNKSA-N O=CC1=CC=C(/C=C/C(=O)OP)N=C1 Chemical compound O=CC1=CC=C(/C=C/C(=O)OP)N=C1 UDEXLEROVMQATR-ONEGZZNKSA-N 0.000 description 1
- PVUKGNBRJFTFNJ-UHFFFAOYSA-N O=CC1=CC=C(Br)N=C1 Chemical compound O=CC1=CC=C(Br)N=C1 PVUKGNBRJFTFNJ-UHFFFAOYSA-N 0.000 description 1
- AGPZPJHWVWZCMG-UHFFFAOYSA-N O=CC1=CC=C(CC(=O)O)C=C1 Chemical compound O=CC1=CC=C(CC(=O)O)C=C1 AGPZPJHWVWZCMG-UHFFFAOYSA-N 0.000 description 1
- NRCCSDVEUWXOMG-UHFFFAOYSA-N O=CC1=CC=C(CCC(=O)O)C=C1 Chemical compound O=CC1=CC=C(CCC(=O)O)C=C1 NRCCSDVEUWXOMG-UHFFFAOYSA-N 0.000 description 1
- KTTOLEBOSHDZRO-UHFFFAOYSA-N [H]C(=O)C1=CC=C(C(C(=O)OP)C(=O)OP)C=C1C Chemical compound [H]C(=O)C1=CC=C(C(C(=O)OP)C(=O)OP)C=C1C KTTOLEBOSHDZRO-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/10—Laxatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/12—Antidiuretics, e.g. drugs for diabetes insipidus
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
Definitions
- the present invention relates to novel benzylpiperazine derivatives having pharmacological activity, processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of various disorders.
- GPR38 is a 7-transmembrane, G-protein coupled receptor, with high affinity for the peptide motilin [Feighner et al., Science 1999, 284, 2184], suggesting that endogenous motilin exerts all or most of its activity via this receptor.
- Motilin is a 22 amino acid peptide found in large amounts within endocrine-like cells of the gastrointestinal tract, and especially in the duodenum-jejunum areas. During fasting, the peptide is known to be associated with the onset of Phase III migrating complex activity within the stomach [Boivin et al., Dig. Dis. Sci. 1992, 37, 1562], suggesting a role in the mechanisms of prokinetic activity. Motilin is also released from the gut during feeding, sham feeding, gastric distension or by oral or intravenous nutrient application [Christofides et al., Gut 1979, 20, 102; Bormans et al., Scand. J. Gastroenterol. 1987, 22, 781], suggesting additional roles for this peptide in the modulation of motility patterns during feeding.
- motilin In animals or in man, motilin has long been known to increase gastrointestinal motility, and promote gastric emptying and intestinal propulsion in an anal direction, during both fasting and fed conditions. This activity is thought to be primarily due to a facilitation of at least the cholinergic excitatory function of the gut [Van Assche et al., Eur. J. Pharmacol. 1997, 337, 267], perhaps also involving the activation of the vagus nerve [Mathis & Malbert, Am. J. Physiol. 1998, 274, G80]. In addition, higher concentrations of motilin directly evoke a small contraction of the muscle [Van Assche et al., Eur. J. Pharmacol. 1997, 337, 267].
- the antibiotic erythromycin was shown to mimic the gastrointestinal activity of motilin, in addition to its previously-described antibiotic properties [see Peeters, in Problems of the Gastrointestinal Tract in Anaesthesia Ed., Herbert M K et al. Springer-Verlag, Berlin, Heidelberg 1999, pp 39-51]. More recently, erythromycin has been shown to activate the GPR38 receptor, confirming its ability to mimic the function of motilin [Carreras et al., Analyt. Biochem. 2002, 300, 146]. In addition, the availability of this non-peptide motilin receptor agonist has allowed at least some clinical studies to be undertaken in order to examine the clinical potential of motilin receptor agonists.
- agonists at the GPR38 receptor will mimic the activity of motilin and find clinical utility in the treatment of gastrointestinal disorders associated with hypomotility, especially the functional bowel disorders such as GERD, functional dyspepsia (FD) and irritable bowel syndrome (IBS).
- the compounds will also be useful for the treatment of other GI conditions where the cause is known and in which GI motility is reduced.
- Such conditions include constipation, caused by various diseases such as those associated with neuropathy, and/or by the administration of other drugs, intestinal pseudo-obstruction, paralytic ileus following surgery or some other manipulation, gastric stasis or hypomotility caused by various diseases such as diabetes and/or by the administration of other drugs.
- agonists active at the GPR38 receptor will, in addition to promoting gastrointestinal motility, facilitate eating behaviours in at least those patients in which some degree of appetite suppression or cachexia is present. Such activity indicates that agonists at this receptor will find clinical utility in the treatment of symptoms associated with—for example—the treatment of cancer or by the presence of the cancer itself.
- motilin receptor agonists In addition to the ability of motilin receptor agonists to promote gastrointestinal motility, the association of motilin gene polymorphism with Crohn's disease [Annese et al., Dig. Dis. Sci. 1998, 43, 715-710] and the changes in motilin receptor density during colitis [Depoortere et al., Neurogastroenterol. Motil. 2001, 13, 55] suggests a utility for agonists at the motilin receptor for the treatment of inflammatory bowel conditions in general.
- GPR38 is also found in regions outside the gastrointestinal tract. These areas include the pituitary, adipose tissue, urinary bladder and certain areas of the brain. The former suggests clinical utility in the promotion of pituitary function, such as the release of growth hormone secretagogues, the presence within adipose tissue again suggests a role in the control of body weight, and the presence within the urinary bladder suggests a role for agonists at this receptor in the treatment of incontinence. The presence of GPR38 within the brain supports the gastrointestinal and feeding utilities already mentioned, but in addition, suggests an involvement of the receptor in a greater spectrum of vagal-hypothalamic functions.
- WO9410185, EP838469, WO9823629, DE19805822, and U.S. Pat. No. 6,165,985 claim erythromycin derivatives targeting GPR38 for use in disorders relating to gastrointestinal motility.
- WO9921846, WO0185694, WO0168620, WO0168621, and WO0168622 disclose a series of small molecule antagonists of the GPR38 receptor.
- JP07138284 and EP807639 disclose peptide agonists.
- JP09249620, WO02092592, WO05027637, US2005065156 and Li et al., (2004, Journal of Medicinal Chemistry, 47(7) p 1704-1708) disclose series of small molecule agonists.
- the present invention therefore provides compounds of formula (I) or pharmaceutically acceptable salts or solvates thereof:
- R 3 When R 3 is substituted, it may have 1, 2 or 3 substituents, each independently selected from halogen, C (1-4) alkyl, C (1-4) alkoxy, C (3-7) cycloalkyl, hydroxy, trifluoromethoxy, trifluoromethyl, nitro, cyano, phenyl, NH 2 , NHR 8 , NR 8 R 9 , NHCOR 8 , NHSO 2 R 8 , C(O)CF 3 , C(O)C (1-4) alkyl, C(O)C (3-7) cycloalkyl, C(O)OC (1-4) alkyl, C(O)OC (3-7) cycloalkyl, OC(O)C (1-4) alkyl, OC(O)C (3-7) cycloalkyl, CONH 2 , CONHR 8 , CONR 8 R 9 , SOR 9 , SO 2 R 9 , OSO 2 R 9 , OSO 2 CF 3 , SO 2 NH 2 ,
- alkyl as a group or part of a group e.g. alkoxy or hydroxyalkyl refers to a straight or branched alkyl group in all isomeric forms.
- C (1-4) alkyl refers to an alkyl group, as defined above, containing at least 1, and at most 4 carbon atoms Examples of such alkyl groups include methyl, ethyl, propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, or tert-butyl, Examples of such alkoxy groups include methoxy, ethoxy, propoxy, isopropoxy, butoxy, iso-butoxy, sec-butoxy and tert-butoxy.
- halogen refers to fluorine (F), chlorine (Cl), bromine (Br), or iodine (I) and the term “halo” refers to the halogen: fluoro (—F), chloro (—Cl), bromo (—Br) and iodo (—I).
- heteroaryl represents a 5 or 6 membered unsaturated ring which comprises one or more heteroatoms.
- heteroaryl represents a 5 membered group it contains a heteroatom selected from O, N or S and may optionally contain a further 1 to 3 nitrogen atoms.
- heteroaryl represents a 6-membered group it contains from 1 to 3 nitrogen atoms.
- Examples of such 5 or 6 membered heteroaryl rings include pyrrolyl, triazolyl, thiadiazolyl, tetrazolyl, imidazolyl, pyrazolyl, isothiazolyl, thiazolyl, isoxazolyl, oxazolyl, oxadiazolyl, furazanyl, furanyl, thienyl, pyridyl, pyrimidinyl, pyrazinyl, pyridazinyl and triazinyl.
- R 3 When R 3 is substituted phenyl it may be substituted by one to two substituents selected from fluoro, cyano, trifluoromethyl and methoxy.
- compounds of formula (I) may exist as stereoisomers.
- the invention extends to all optical isomers such as stereoisomeric forms of the compounds of formula (I) including enantiomers, diastereoisomers and mixtures thereof, such as racemates.
- the different stereoisomeric forms may be separated or resolved one from the other by conventional methods or any given isomer may be obtained by conventional stereoselective or asymmetric syntheses.
- Preferred compounds of formula (I) wherein R 1 and R 2 are both methyl are those wherein the piperazine C* carbons have the cis configuration.
- Suitable compounds of the invention are:
- the compounds of formula (I) can form acid addition salts thereof. It will be appreciated that for use in medicine the salts of the compounds of formula (I) should be pharmaceutically acceptable. Suitable pharmaceutically acceptable salts will be apparent to those skilled in the art and include those described in J. Pharm. Sci., 1977, 66, 1-19, such as acid addition salts formed with inorganic acids e.g. hydrochloric, hydrobromic, sulfuric, nitric or phosphoric acid; and organic acids e.g. succinic, maleic, acetic, fumaric, citric, tartaric, benzoic, p-toluenesulfonic, methanesulfonic or naphthalenesulfonic acid. Certain of the compounds of formula (I) may form acid addition salts with one or more equivalents of the acid.
- the present invention includes within its scope all possible stoichiometric and non-stoichiometric forms.
- the compounds of formula (I) may be prepared in crystalline or non-crystalline form, and, if crystalline, may optionally be hydrated or solvated.
- This invention includes within its scope stoichiometric hydrates or solvates as well as compounds containing variable amounts of water and/or solvent.
- this invention provides processes for the preparation of a compound of formula (I)
- A is phenyl and X is CH 2 or a pharmaceutically acceptable salt or solvate thereof, which process comprises reacting of a compound of formula (II)
- R 1 and R 2 are as defined in formula (I) and Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ), with a compound of formula (III)
- Y and R 3 are as defined in formula (I), using reaction conditions suitable for a reductive alkylation, for example in the presence of a reducing agent such as sodium tri(acetoxy)borohydride in a suitable solvent such as dichloromethane or 1,2-dichloroethane.
- a reducing agent such as sodium tri(acetoxy)borohydride
- a suitable solvent such as dichloromethane or 1,2-dichloroethane.
- a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexylcarbodiimide (DCC), in a suitable solvent such as dichloromethane, dimethylformamide or mixtures thereof.
- a compound of formula (III) may be prepared by reacting a compound of formula (IV) with an activated derivative of a compound of formula (V), such as an acid chloride, using general methods described in J. March, Advanced Organic Chemistry, 4 th Edition, J Wiley & Sons, 1992, p. 417-418.
- a reducing agent such as sodium tri(acetoxy)borohydride
- a suitable aryl halide such as (1-tert-butoxycarbonyl)-4-aminopiperidine
- a suitable catalyst system such as palladium (II) acetate/BINAP
- solvent such as 1,4-dioxane
- a suitable phenol derivative such as 1-(tert-butoxycarbonyl)-4-hydroxypiperidine
- triphenylphosphine and diisopropylazodicarboxylate in a solvent such as tetrahydrofuran
- the present invention provides a further process for the preparation of a compound of formula (I) wherein A is phenyl and X is CH 2 or a pharmaceutically acceptable salt or solvate thereof, which process comprises reacting a compound of formula (VI)
- R 1 and R 2 are as defined in formula (I) and Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ), with a compound of formula (IV) in the presence of a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexylcarbodiimide (DCC), in a suitable solvent such as dichloromethane, dimethylformamide or mixtures thereof.
- a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexylcarbodiimide (DCC)
- a compound of formula (I) wherein A is phenyl and X is CH 2 or a pharmaceutically acceptable salt or solvate thereof may be prepared by a process which comprises reacting an activated derivative of a compound of formula (VI), such as an acid chloride, with a compound of formula (IV) using general methods described in J. March, Advanced Organic Chemistry, 4 th Edition, J Wiley & Sons, 1992, p. 417-418
- R 1 and R 2 are as defined in formula (I)
- Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ) and P is a suitable alkyl group such as methyl or ethyl, using aqueous sodium hydroxide in a suitable solvent such as 1,4-dioxane followed by acidification and decarboxylation by heating in a suitable solvent such as toluene.
- BOC tert-butyloxycarbonyl
- CBZ benzyloxycarbonyl
- L is a suitable leaving group such as a halogen, for example bromine
- Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ), with a suitable dialkyl malonate such as diethyl malonate under palladium catalysis in a suitable solvent such as 1,4-dioxane at reflux using a method similar to that described in S. L. Buchwald et al, J. Am. Chem. Soc., 2000, vol 122, p 1360-1370
- L is halogen, with a compound of formula (II), using reaction conditions suitable for a reductive amination, for example in the presence of a reducing agent such as sodium tri(acetoxy)borohydride in a suitable solvent such as dichloromethane or 1,2-dichloroethane.
- a reducing agent such as sodium tri(acetoxy)borohydride
- a suitable solvent such as dichloromethane or 1,2-dichloroethane.
- R 1 and R 2 are as defined in formula (I)
- Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ)
- P is a suitable alkyl group such as methyl, using a suitable base such as aqueous sodium hydroxide in a suitable solvent such as tetrahydrofuran or 1,4-dioxane.
- P is a suitable alkyl group such as methyl and L is a suitable leaving group such as a halogen, for example bromine, in the presence of a suitable base such as diisopropylethylamine in a suitable solvent such as dimethylformamide.
- the present invention provides a process for the preparation of a compound of formula (I) wherein A is substituted phenyl and X is CH 2 or a pharmaceutically acceptable salt or solvate thereof, which process comprises reacting a compound of formula (XIII),
- R 1 and R 2 are as defined in formula (I), Z is C (1-4) alkoxy and Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ) with a compound of formula (IV) in the presence of a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N-dicyclohexyl carbodiimide (DCC), in a suitable solvent such as dichloromethane, dimethylformamide or mixtures thereof.
- a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N-dicyclohexyl carbodiimide (DCC)
- a suitable solvent such as dichloromethane, dimethylformamide or mixtures thereof.
- a compound of formula (I) wherein A is substituted phenyl and X is CH 2 or a pharmaceutically acceptable salt or solvate thereof may be prepared by a process which comprises reacting an activated derivative of a compound of formula (XIII), such as an acid chloride, with a compound of formula (IV) using general methods described in J. March, Advanced Organic Chemistry, 4 th Edition, J Wiley & Sons, 1992, p. 417-418.
- R 1 and R 2 are as defined in formula (I)
- Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ)
- Z is C (1-4) alkoxy
- P is a suitable alkyl group such as methyl or ethyl, using aqueous sodium hydroxide followed by acidification and decarboxylation by heating in a suitable solvent such as tetrahydrofuran or 1,4-dioxane.
- Z is C (1-4) alkoxy and P is a suitable alkyl group such as methyl or ethyl, with a compound of formula (II) using reaction conditions suitable for a reductive amination, for example in the presence of a reducing agent such as sodium tri(acetoxy)borohydride in a suitable solvent such as dichloromethane or 1,2-dichloroethane.
- a reducing agent such as sodium tri(acetoxy)borohydride
- a suitable solvent such as dichloromethane or 1,2-dichloroethane.
- Z is C (1-4) alkoxy and P is alkyl such as ethyl, using a suitable aqueous acid, such as dilute hydrochloric acid, in a suitable solvent such as tetrahydrofuran.
- L is halogen such as bromine and Z is C (1-4) alkoxy
- a suitable dialkyl malonate such as diethyl malonate under palladium catalysis in a suitable solvent such as 1,4-dioxane at reflux using a method similar to that described in S. L. Buchwald et al, J. Am. Chem. Soc., 2000, vol 122, p 1360-1370.
- the present invention provides a process for the preparation of a compound of formula (I) wherein A is phenyl and X is CMe 2 or a pharmaceutically acceptable salt or solvate thereof, which process comprises reacting a compound of formula (XVIII)
- R 1 and R 2 are as defined in formula (I) and Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ) with a compound of formula (IV) in the presence of a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexylcarbodiimide (DCC), in a suitable solvent such as dichloromethane, dimethylformamide or mixtures thereof.
- a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ) with a compound of formula (IV) in the presence of a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexy
- a compound of formula (I) wherein A is phenyl and X is CMe 2 or a pharmaceutically acceptable salt or solvate thereof may be prepared by a process which comprises reacting an activated derivative of a compound of formula (XVIII), such as an acid chloride, with a compound of formula (IV) using general methods described in J. March, Advanced Organic Chemistry, 4 th Edition, J Wiley & Sons, 1992, p. 417-418.
- R 1 and R 2 are as defined in formula (I)
- Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ)
- P is a suitable alkyl group such as methyl, using a suitable base such as aqueous lithium hydroxide in a suitable solvent such as 1,4-dioxane.
- P is a suitable alkyl group such as methyl using a procedure similar to that described in J. F. Hartwig et al, J. Am. Chem. Soc., 2002, vol 124, p 12557-12565.
- the reaction may be carried out in the presence of a suitable base such as lithium di(cyclohexyl)amide, a suitable catalyst system such as bis(dibenzylidene) palladium (0)/tri(tert-butyl)phosphine and in a suitable solvent such as toluene.
- a suitable base such as lithium di(cyclohexyl)amide
- a suitable catalyst system such as bis(dibenzylidene) palladium (0)/tri(tert-butyl)phosphine
- a suitable solvent such as toluene.
- the present invention provides a process for the preparation of a compound of formula (I) wherein A is phenyl and X is CHMe or a pharmaceutically acceptable salt or solvate thereof, which process comprises reacting a compound of formula (XXI)
- R 1 and R 2 are as defined in formula (I) and Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ) with a compound of formula (IV) in the presence of a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexylcarbodiimide (DCC), in a suitable solvent such as dichloromethane, dimethylformamide or mixtures thereof.
- a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ) with a compound of formula (IV) in the presence of a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexy
- a compound of formula (I) wherein A is phenyl and X is CHMe or a pharmaceutically acceptable salt or solvate thereof may be prepared by a process which comprises reacting an activated derivative of a compound of formula (XXI), such as an acid chloride, with a compound of formula (IV) using general methods described in J. March, Advanced Organic Chemistry, 4 th Edition, J Wiley & Sons, 1992, p. 417-418.
- R 1 and R 2 are as defined in formula (I)
- Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ) and P is a suitable alkyl group such as methyl or ethyl, using aqueous sodium hydroxide followed by acidification and decarboxylation by heating in a suitable solvent such as 1,4-dioxane or tetrahydrofuran.
- BOC tert-butyloxycarbonyl
- CBZ benzyloxycarbonyl
- R 1 and R 2 are as defined in formula (I)
- Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ)
- P is a suitable alkyl group such as methyl or ethyl, using standard alkylation conditions.
- a suitable base such as sodium hydride
- a suitable methylating agent such as iodomethane
- the present invention provides a process for the preparation of a compound of formula (I) wherein A is phenyl and X is CH 2 CH 2 or a pharmaceutically acceptable salt or solvate thereof, which process comprises reacting a compound of formula (XXIII)
- Y and R 3 are as defined in formula (I), with a compound of formula (II) using reaction conditions suitable for a reductive amination, for example in the presence of a reducing agent such as sodium tri(acetoxy)borohydride in a suitable solvent such as dichloromethane or 1,2-dichloroethane.
- a reducing agent such as sodium tri(acetoxy)borohydride
- a suitable solvent such as dichloromethane or 1,2-dichloroethane.
- a compound of formula (IV) in the presence of a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexylcarbodiimide (DCC), in a suitable solvent such as dichloromethane, dimethylformamide or mixtures thereof.
- a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexylcarbodiimide (DCC)
- a suitable solvent such as dichloromethane, dimethylformamide or mixtures thereof.
- a compound of formula (XXIII) may be prepared by reacting a compound of formula (IV) with an activated derivative of a compound of formula (XXIV), such as an acid chloride, using general methods described in J. March, Advanced Organic Chemistry, 4 th Edition, J Wiley & Sons, 1992, p. 417-418.
- the present invention provides a process for the preparation of a compound of formula (I) wherein A is 2,5-pyridyl and X is CH 2 CH 2 or a pharmaceutically acceptable salt or solvate thereof, which process comprises hydrogenation of a compound of formula (XXV),
- R 1 and R 2 are as defined in formula (I) and Q is a suitable protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ) in the presence of a suitable catalyst such as palladium black and in a suitable solvent such as methanol.
- BOC tert-butyloxycarbonyl
- CBZ benzyloxycarbonyl
- R 1 and R 2 are as defined in formula (I) and Q is a suitable protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ), with a compound of formula (IV) in the presence of a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexylcarbodiimide (DCC), in a suitable solvent such as dichloromethane, dimethylformamide or mixtures thereof.
- BOC tert-butyloxycarbonyl
- CBZ benzyloxycarbonyl
- a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexylcarbodiimide (DCC)
- a suitable solvent such as dichloromethane, di
- a compound of formula (XXV) may be prepared by reacting a compound of formula (IV) with an activated derivative of a compound of formula (XXVI), such as an acid chloride, using general methods described in J. March, Advanced Organic Chemistry, 4 th Edition, J Wiley & Sons, 1992, p. 417-418.
- R 1 and R 2 are as defined in formula (I)
- Q is a suitable protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ)
- P is a suitable alkyl group such as methyl, using a suitable base such as aqueous lithium hydroxide in a suitable solvent such as 1,4-dioxane.
- P is a suitable alkyl group such as methyl
- a compound of formula (II) using reaction conditions suitable for a reductive amination, for example in the presence of a reducing agent such as sodium tri(acetoxy)borohydride in a suitable solvent such as dichloromethane or 1,2-dichloroethane.
- a reducing agent such as sodium tri(acetoxy)borohydride
- a suitable solvent such as dichloromethane or 1,2-dichloroethane.
- a suitable alkyl acrylate such as methyl acrylate
- a suitable catalyst system such as allyl palladium (II) chloride dimer/tri(o-tolyl)phosphine
- a suitable base such as sodium acetate.
- a suitable solvent is dimethylformamide.
- Standard protection and deprotection techniques such as those described in Greene T. W. Protective groups in organic synthesis, New York, Wiley (1981), can be used.
- primary amines can be protected as phthalimide, trifluoroacetyl, benzyl, tert-butyloxycarbonyl, benzyloxycarbonyl or trityl derivatives.
- Carboxylic acid groups can be protected as esters.
- Aldehyde or ketone groups can be protected as acetals, ketals, thioacetals or thioketals.
- protecting groups such as tert-butyloxycarbonyl may be removed using an acid such as hydrochloric or trifluororoacetic acid in a suitable solvent such as dichloromethane, diethylether, 1,4-dioxane, isopropanol or mixtures thereof.
- compositions may be prepared conventionally by reaction with the appropriate acid or acid derivative.
- the present invention also provides compounds of formula (III), (VI), (VII), (X), (XIII), (XIV), (XVIII), (XIX), (XXI), (XXII), (XXIII), (XXV), (XXVI) and (XXVII) as shown above wherein Y, R 1 , R 2 and R 3 are as defined for formula (I), Q is hydrogen or a suitable protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ) and P is a suitable alkyl group such as ethyl.
- BOC tert-butyloxycarbonyl
- CBZ benzyloxycarbonyl
- P is a suitable alkyl group such as ethyl.
- potencies and efficacies of the compounds of this invention for GPR38 can be determined by FLIPR assay performed on the human cloned receptor as described herein.
- Compounds of formula (I) have demonstrated partial or full agonist activity at the GPR38 receptor, using the FLIPR (FLourometric Imaging Plate Reader) functional assay described herein.
- Compounds of formula (I) and their pharmaceutically acceptable salts are therefore of use in the treatment of conditions or disorders which are mediated via the GPR38 receptor.
- the compounds of formula (I) and their pharmaceutically acceptable salts are of use in the treatment of certain gastrointestinal disorders such as gastroesophageal reflux disorders, functional dyspepsia, irritable bowel syndrome, constipation, intestinal pseudo-obstruction, paralytic ileus following surgery or other manipulation, emesis, gastric stasis or hypomotility caused by various diseases such as diabetes and/or by the administration of other drugs, Crohn's disease, colitis, cachexia associated with advanced diseases such as cancer and/or the treatment thereof, appetite/metabolism related cachexia and other disorders such as incontinence (herein after referred to as the “Disorders of the Invention”).
- treatment includes prophylaxis as well as alleviation of established symptoms.
- the invention also provides a compound of formula (I) or a pharmaceutically acceptable salt thereof, for use as a therapeutic substance, in particular in the treatment of the conditions or disorders mediated via the GPR38 receptor.
- the invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof for use as a therapeutic substance in the treatment of gastrointestinal disorders such as gastroesophageal reflux disorders, functional dyspepsia, irritable bowel syndrome, constipation, intestinal pseudo-obstruction, paralytic ileus following surgery or other manipulation, emesis, gastric stasis or hypomotility caused by various diseases such as diabetes and/or by the administration of other drugs, Crohn's disease, colitis, cachexia associated with advanced diseases such as cancer and/or the treatment thereof, appetite/metabolism related cachexia and other disorders such as incontinence.
- the invention further provides a method of treatment of conditions or disorders in mammals including humans which can be mediated via the GPR38 receptor, which comprises administering to the sufferer a therapeutically safe and effective amount of
- the invention provides for the use of a compound of formula (I) or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for use in the treatment of the conditions or disorders mediated via the GPR38 receptor
- the present invention also provides a pharmaceutical composition, which comprises a compound of formula (I) or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient.
- the present invention provides a process for preparing a pharmaceutical composition, the process comprising mixing a compound of formula (I) or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier or excipient.
- a pharmaceutical composition of the invention which may be prepared by admixture, suitably at ambient temperature and atmospheric pressure, is usually adapted for oral, parenteral or rectal administration and, as such, may be in the form of tablets, capsules, oral liquid preparations, powders, granules, lozenges, reconstitutable powders, injectable or infusible solutions or suspensions or suppositories. Orally administrable compositions are generally preferred.
- Tablets and capsules for oral administration may be in unit dose form, and may contain conventional excipients, such as binding agents (e.g. pregelatinised maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose); fillers (e.g. lactose, microcrystalline cellulose or calcium hydrogen phosphate); tabletting lubricants (e.g. magnesium stearate, talc or silica); disintegrants (e.g. potato starch or sodium starch glycollate); and acceptable wetting agents (e.g. sodium lauryl sulphate).
- binding agents e.g. pregelatinised maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose
- fillers e.g. lactose, microcrystalline cellulose or calcium hydrogen phosphate
- tabletting lubricants e.g. magnesium stearate, talc or silica
- disintegrants e.g. potato starch or sodium starch glycollate
- Oral liquid preparations may be in the form of, for example, aqueous or oily suspension, solutions, emulsions, syrups or elixirs, or may be in the form of a dry product for reconstitution with water or other suitable vehicle before use.
- Such liquid preparations may contain conventional additives such as suspending agents (e.g. sorbitol syrup, cellulose derivatives or hydrogenated edible fats), emulsifying agents (e.g. lecithin or acacia), non-aqueous vehicles (which may include edible oils e.g. almond oil, oily esters, ethyl alcohol or fractionated vegetable oils), preservatives (e.g.
- Preparations for oral administration may be suitably formulated to give controlled release of the active compound.
- fluid unit dosage forms are prepared utilising a compound of the invention or pharmaceutically acceptable salt thereof and a sterile vehicle.
- Formulations for injection may be presented in unit dosage form e.g. in ampoules or in multi-dose, utilising a compound of the invention or pharmaceutically acceptable salt thereof and a sterile vehicle, optionally with an added preservative.
- the compositions may take such forms as suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilising and/or dispersing agents.
- the active ingredient may be in powder form for constitution with a suitable vehicle, e.g. sterile pyrogen-free water, before use.
- the compound depending on the vehicle and concentration used, can be either suspended or dissolved in the vehicle.
- the compound can be dissolved for injection and filter sterilised before filling into a suitable vial or ampoule and sealing.
- adjuvants such as a local anaesthetic, preservatives and buffering agents are dissolved in the vehicle.
- the composition can be frozen after filling into the vial and the water removed under vacuum.
- Parenteral suspensions are prepared in substantially the same manner, except that the compound is suspended in the vehicle instead of being dissolved, and sterilisation cannot be accomplished by filtration.
- the compound can be sterilised by exposure to ethylene oxide before suspension in a sterile vehicle.
- a surfactant or wetting agent is included in the composition to facilitate uniform distribution of the compound.
- Lotions may be formulated with an aqueous or oily base and will in general also contain one or more emulsifying agents, stabilising agents, dispersing agents, suspending agents, thickening agents, or colouring agents. Drops may be formulated with an aqueous or non-aqueous base also comprising one or more dispersing agents, stabilising agents, solubilising agents or suspending agents. They may also contain a preservative.
- the compounds of the invention may also be formulated in rectal compositions such as suppositories or retention enemas, e.g. containing conventional suppository bases such as cocoa butter or other glycerides.
- the compounds of the invention may also be formulated as depot preparations. Such long acting formulations may be administered by implantation (for example subcutaneously or intramuscularly) or by intramuscular injection.
- the compounds of the invention may be formulated with suitable polymeric or hydrophobic materials (for example as an emulsion in an acceptable oil) or ion exchange resins, or as sparingly soluble derivatives, for example, as a sparingly soluble salt.
- the compounds of the invention may be formulated as solutions for administration via a suitable metered or unitary dose device or alternatively as a powder mix with a suitable carrier for administration using a suitable delivery device.
- compounds of formula (I) may be formulated for oral, buccal, parenteral, topical (including ophthalmic and nasal), depot or rectal administration or in a form suitable for administration by inhalation or insufflation (either through the mouth or nose).
- the compounds of the invention may be formulated for topical administration in the form of ointments, creams, gels, lotions, pessaries, aerosols or drops (e.g. eye, ear or nose drops).
- Ointments and creams may, for example, be formulated with an aqueous or oily base with the addition of suitable thickening and/or gelling agents.
- Ointments for administration to the eye may be manufactured in a sterile manner using sterilised components.
- the composition may contain from 0.1% to 99% by weight, preferably from 10 to 60% by weight, of the active material, depending on the method of administration.
- the dose of the compound used in the treatment of the aforementioned disorders will vary in the usual way with the seriousness of the disorders, the weight of the sufferer, and other similar factors.
- suitable unit doses may be 0.05 to 1000 mg, 1.0 to 500 mg or 1.0 to 200 mg and such unit doses may be administered more than once a day, for example two or three times a day. Such therapy may extend for a number of weeks or months.
- the compounds of the present invention may be used in combination preparations.
- the compounds of the invention may be used in combination with one or more compounds with activity in reducing gastric acid; one or more compounds with activity in reducing gastro-esophageal reflux; one or more compounds with activity in reducing esophago-gastric irritancy or inflammation, especially when used to alleviate erosive or non-erosive esophagitis; one or more compounds with analgesic activity; and/or one or more compounds with mixed activity on motility and pain.
- Examples of compounds with activity in reducing gastric acid include H2 receptor antagonists, acid pump antagonists and proton pump inhibitors.
- Examples of compounds with activity in reducing gastro-esophageal reflux include agonists at GABA-B.
- Examples of compounds with analgesic activity include compounds active at Neurokinin receptors (NK1, 2, 3), TRPV1 and sodium-channels.
- Examples of compounds with mixed activity on motility and pain include CRF2 antagonists, 5-HT3 antagonists or octreotide or other molecules active at sst2 receptors.
- the column used is a Waters Atlantis, the dimensions of which are 4.6 mm ⁇ 50 mm.
- the stationary phase particle size is 3 ⁇ m.
- the generic method used has a 5 minute runtime.
- the above method has a flow rate of 3 ml/mins
- Open Access Mass Directed Prep instruments consist of the following:
- the column used is typically a Supelco LCABZ++ column whose dimensions are 20 mm internal diameter by 100 mm in length.
- the stationary phase particle size is 5 ⁇ m.
- One of five methods may be used depending on the analytical retention time of the compound of interest.
- the title compound was prepared from [4-(bromomethyl)phenyl]acetic acid and hexamethylenetetramine using a method similar to that described in J. March, Advanced Organic Chemistry, 4 th Edition, J Wiley & Sons, 1992, p. 1194.
- the title compound was prepared from 1,1-dimethylethyl 4-oxo-1-piperidinecarboxylate and 3,4-difluoroaniline using a method similar to that described for D1 although the crude product was purified by chromatography.
- the title compound was prepared from D9a using a method similar to that described for D2 although the reaction was heated at 80° C.
- the title compound was prepared from 1,1-dimethylethyl 4-amino-1-piperidinecarboxylate and 4-bromobenzonitrile using a method similar to that described for D10a
- the title compound was prepared from D11a using a method similar to that described for D10b although purification by chromatography was also carried out.
- the title compound was prepared from 1,1-dimethylethyl 4-oxo-1-piperidinecarboxylate and 4-fluoro-3-methoxyaniline using a method similar to that described for D1.
- the title compound was prepared from D12a using a method similar to that described for D2 although the reaction was heated at 80° C.
- the title compound may be prepared using a method similar to that described in L. C Blumberg, M. F. Brown, M. M. Hayward and C. S. Poss, PCT Int. Appl., WO 2004009550.
- the title compound was prepared from 1,1-dimethylethyl 4-oxo-1-piperidinecarboxylate and 4-trifluoromethylaniline using a method similar to that described for D20
- the title compound was prepared from D22 using a method similar to that described for D21.
- the title compound was prepared from phenylmethyl 1-piperazinecarboxylate and 4-bromobenzaldehyde using a method to that described for D6
- the title compound was prepared from D24 using a method similar to that described for D7.
- the title compound was prepared from 4-hydroxybenzonitrile and 1,1-dimethylethyl 4-hydroxy-1-piperidinecarboxylate using a method similar to that described for D13.
- the title compound was prepared from D30 using a method similar to that described for D14.
- the title compound may be prepared using the method described in A. Tromelin, P. Demerseman, R. Royer, P. Gayral and J. Fourniat, European Journal of Medicinal Chemistry 1986, 21(5), 397-402.
- the title compound was prepared from D34 and 1,1-dimethylethyl (2S)-2-methyl-1-piperazinecarboxylate using a method similar to that described for D6.
- the title compound was prepared from D35 using a method similar to that described for D26.
- the title compound was prepared from 5-bromo-2-fluorobenzonitrile and 1,1-dimethylethyl 4-amino-1-piperidinecarboxylate using a method similar to that described for D10a.
- the title compound was prepared from D38 using a method similar to that described for D10b.
- the title compound was prepared from D8 and D39 using a method similar to that described for D29 although the reaction time was overnight and an aqueous work-up (DCM/water) was carried out prior to chromatography.
- Step 1 (2E)-3-(4-formylphenyl)-2-propenoic acid (2.55 g) was dissolved in EtOH (250 ml) and hydrogenated at atmospheric pressure with 10% Pd/C (0.8 g) as catalyst. After 5 h the reaction mixture was filtered and concentrated to give a 1:1 mixture of 3-[4-(hydroxymethyl)phenyl]propanoic acid and 3-(4-methylphenyl)propanoic acid (2.43 g).
- Step 2 The acid mixture from step 1 (500 mg), N-[3-(dimethylamino)propyl]-N -(ethylcarbodiimide hydrochloride (723 mg, 3.78 mmol), 1-hydroxybenzotriazole (578 mg, 3.78 mmol) in DMF (10 ml) was treated with D2 (561 mg, 2.9 mmol) and the mixture stirred at room temperature for 2 h. The DMF was removed in vacuo and EtOAc and water were added. The aqueous was extracted with EtOAc and the combined organics were washed with saturated aq.
- Step 3 This whole was dissolved in DCM (20 ml) and treated with manganese dioxide (2 g). After stirring overnight, further manganese dioxide was added (5 g) and stirring continued for 30 mins. The mixture was filtered, concentrated and purified by chromatography (10-90% EtOAc/pentane) to give the title compound as a yellow gum (282 mg). MS (ES): MH + 355.
- the title compound was prepared from D5b using a method similar to that described for D41.
- the title compound was prepared from D43 using a method similar to that described for D7.
- the title compound was prepared from D50 using a method similar to that described for D48 although the reaction time was 3 h.
- the title compound was prepared from D51 and D5b using a method similar to that described for D37.
- the title compound was prepared from methyl (3-chloro-4-formylphenyl)acetate (Epple, R. et al., PCT Int. Appl. WO2005116000) and 1,1-dimethylethyl (2S)-2-methyl-1-piperazinecarboxylate hydrochloride using a method similar to that described for D6 with the addition of triethylamine (1.1 eq) to the reaction mixture and a reaction time of ⁇ 3 days.
- the title compound was prepared from D53 using a method similar to that described for D48 with a reaction time of 4 h.
- the title compound was prepared from D54 and D5b using a procedure similar to that described for D37 with the reaction carried out under an argon atmosphere.
- 3-Fluoroaniline 28.38 ml, 0.296 mol was added to a solution of 4-oxo-1-piperidine carboxylate (60 g, 0.302 mol) in 1,2-DCE (600 ml) and the mixture stirred for 15 mins.
- Sodium tri(acetoxy)borohydride (83 g, 0.392 mol) was added gradually over 5 mins and the mixture stirred for 5.5 hrs then poured into a mixture of 2 MHCl (100 ml), water (200 ml) and ice (1 l). The phases were separated and the aqueous phase extracted with DCM (200 ml).
- the aqueous solution was diluted with tert-butylmethyl ether (TBME, 250 ml), the mixture was stirred for 1 min and basified to pH 12-14 by cautious addition of 32% w/w aqueous NaOH (140 g, 100 ml), keeping the temperature between 30 and 35° C.
- the layers were separated and the aqueous extracted with fresh TBME (250 ml).
- the combined organic extracts were washed at 25 to 35° C. with 20% w/v aq. NaCl (200 ml) the aqueous layer separated off and the organic solution distilled down at atmospheric pressure to a final volume of about 200 ml and cooled to 50° C.
- Iso-octane (250 ml) was added slowly at 45-50° C. and the heating bath was removed and the reaction mixture cooled to 20-25° C. The solution was stirred at 20-25° C. overnight.
- Iso-octane (250 ml) was added, the slurry heated to 40° C. and distilled in vacuo down to a final volume of 250 ml maintaining the temperature between 30 and 40° C. The final slurry was cooled to 0-5° C. (in ice-water), stirred for 40 min, filtered, the solids washed with iso-octane (2 ⁇ 100 ml) and dried in vacuo at 44° C. for 3 hrs to give the title product (33.5 g).
- Carbonyldiimidazole (CDI, 53 g, 0.33 mol) was added to the dry solution from D59 (cooled to room temperature) in two portions with 15 min after each addition. The resulting mixture was warmed to 62° C. and stirred for 15 min. D58 (63.5 g, 0.33 mol) was added in one portion causing a minor exothermic reaction warming the contents to 68° C. The mixture was cooled to 62° C. and stirred for 2 h then cooled to 0° C. over 2 hr and held at 0° C. overnight. The final slurry was filtered, the solids washed with ice-cold MIBK (3 ⁇ 75 ml), dried in vacuo at 50° C.
- CDI Carbonyldiimidazole
- the organic solution was distilled down at atmospheric pressure to a final volume of 200 ml and diluted with fresh i-PrOAc (100 ml, 5 vol).
- the solution was heated to reflux, filtered hot through a filter paper and distilled down at atmospheric pressure to a final volume of 200 ml.
- the solution was then cooled slowly over 1 h to 30° C. and the resulting slurry was cooled to 5° C. and stirred for 45 min.
- the solid was collected by filtration, washed with chilled i-PrOAc (2 ⁇ 2 vol) and dried in vacuo overnight to give the title product (12.63 g).
- E3-E11 were prepared from D8 and the amines indicated in the table using methods similar to that described for Example 2, although MP-carbonate was used in place of Si-carbonate in the amide formation step and palladium black was used in place of 10% Pd/C in the deprotection step.
- E12 was prepared from D26 and the amine indicated in the table using a method similar to that described for Example 2, although MP-carbonate was used in place of Si-carbonate in the amide formation step and palladium black was used in place of 10% Pd/C in the deprotection step.
- E14-E20 were prepared from D28 and the amines indicated in the table using methods similar to that described for Example 2, although MP-carbonate was used in place of Si-carbonate in the amide formation step and palladium black was used in place of 10% Pd/C in the deprotection step.
- E28 was prepared from D46 and D5b using a method similar to that described for Example 27.
- CHO-K1 cells stably expressing the GPR38 receptor were seeded (10,000 cells/well) into poly-D-lysine coated 384-well black-wall, clear-bottom microtitre plates (Greiner). On the day of assay, media was aspirated from cell plates using a cell washer (leaving 10 ul of media).
- FLIPR FLuorometric Imaging Plate Reader
- Master compound plates were prepared in 100% DMSO. A top concentration of 3 mM was used (giving 12 ⁇ M final concentration in assay) and this was serially diluted 1 in 4. 1 ul from the master plate was transferred to a daughter plate, to which 50 ⁇ l of compound dilution buffer (Tyrodes+1 mg/ml BSA+1.5 mM CaCl 2 ) was added. In the FLIPR, 10 ul of test compound was added to the cells and changes in fluorescence measured over a 1 minute timeframe. Maximum change in fluorescence over baseline was used to determine agonist response and concentration response curves were constructed, using a 4-parameter logistic equation.
- Exemplified compounds of the invention have a pEC50>6.5 in the FLIPR assay
Abstract
Description
- A is phenyl or a 6-membered heteroaryl ring, optionally substituted with halogen, C(1-4)alkyl or C(1-4)alkoxy;
- R1 and R2 are independently H or C(1-4) alkyl;
- R3 is optionally substituted phenyl or optionally substituted 5 or 6 membered heteroaryl;
- X is (CR4R5)n;
- n is 1 or 2;
- Y is NH, O or CH2;
- R4 and R5 are independently selected from hydrogen and C(1-4) alkyl.
- A is phenyl or pyridyl;
- R1 is hydrogen or methyl;
- R2 is hydrogen or methyl;
- R3 is optionally substituted phenyl;
- Y is NH or O;
- X is (CR4R5)n;
- n is 1 or 2; and
- R4 and R5 are independently hydrogen or methyl.
- A is phenyl;
- R1 is hydrogen or methyl;
- R2 is hydrogen or methyl
- R3 is optionally substituted phenyl:
- Y is NH or O: and
- X is (CR4R5)n;
- n is 1 or 2; and
- R4 and R5 are both hydrogen.
- 1-[(4-{[(3R,5S)-3,5-dimethyl-1-piperazinyl]methyl}phenyl)acetyl]-N-(4-fluorophenyl)-4-piperidinamine (E1)
- N-(3-fluorophenyl)-1-[(4-{[(3S)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-4-piperidinamine (E2)
- N-(4-fluorophenyl)-1-[(4-{[(3S)-3-methyl-1-piperazinyl]methyl}-phenyl)acetyl]-4-piperidinamine (E3)
- 3-({1-[(4-{[(3S)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-4-piperidinyl}amino)benzonitrile (E4)
- 4-({1-[(4-{[(3S)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-4-piperidinyl}amino)benzonitrile (E5)
- N-(3,4-difluorophenyl)-1-[(4-{[(3S)-3-methyl-1-piperazinyl]methyl}-phenyl)acetyl]-4-piperidinamine (E6)
- N-[4-fluoro-3-(methyloxy)phenyl]-1-[(4-{[(3S)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-4-piperidinamine (E7)
- (3S)-1-{[4-(2-{4-[(4-fluorophenyl)oxy]-1-piperidinyl}-2-oxoethyl)phenyl]methyl}-3-methylpiperazine (E8)
- (3S)-1-{[4-(2-{4-[(3-fluorophenyl)oxy]-1-piperidinyl}-2-oxoethyl)phenyl]methyl}-3-methylpiperazine (E9)
- 1-[(4-{[(3S)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-N-[3-(trifluoromethyl)phenyl]-4-piperidinamine (E10)
- 1-[(4-{[(3S)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-N-[4-(trifluoromethyl)phenyl]-4-piperidinamine (E11)
- N-(3-fluorophenyl)-1-{[4-(1-piperazinylmethyl)phenyl]acetyl}-4-piperidinamine (E12)
- N-(3-fluorophenyl)-1-[(4-{[(3R)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-4-piperidinamine (E13)
- N-(3,4-difluorophenyl)-1-[(4-{[(3R)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-4-piperidinamine (E14)
- (3R)-1-{[4-(2-{4-[(4-fluorophenyl)oxy]-1-piperidinyl}-2-oxoethyl)phenyl]methyl}-3-methylpiperazine (E15)
- (3R)-1-{[4-(2-{4-[(3-fluorophenyl)oxy]-1-piperidinyl}-2-oxoethyl)phenyl]methyl}-3-methylpiperazine (E16)
- 4-({1-[(4-{[(3R)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-4-piperidinyl}oxy)benzonitrile (E17)
- 4-({1-[(4-{[(3R)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-4-piperidinyl}amino)benzonitrile (E18)
- 3-({1-[(4-{[(3R)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-4-piperidinyl}amino)benzonitrile (E19)
- 1-[(4-{[(3R)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-N-[3-(trifluoromethyl)phenyl]-4-piperidinamine (E20)
- N-(3-fluorophenyl)-1-[(3-(methyloxy)-4-{[(3S)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-4-piperidinamine (E21)
- 2-fluoro-5-({1-[(4-{[(3S)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-4-piperidinyl}amino)benzonitrile (E22)
- 1-[3-(4-{[(3R,5S)-3,5-dimethyl-1-piperazinyl]methyl}phenyl)propanoyl]-N-(4-fluorophenyl)-4-piperidinamine (E23)
- 1-[3-(4-{[(3R,5S)-3,5-dimethyl-1-piperazinyl]methyl}phenyl)propanoyl]-N-(3-fluorophenyl)-4-piperidinamine (E24)
- N-(4-fluorophenyl)-1-[3-(4-{[(3S)-3-methyl-1-piperazinyl]methyl}phenyl) propanoyl]-4-piperidinamine (E25)
- N-(3-fluorophenyl)-1-[3-(4-{[(3S)-3-methyl-1-piperazinyl]methyl}phenyl)propanoyl]-4-piperidinamine (E26)
- 1-[2-(4-{[(3R,5S)-3,5-dimethyl-1-piperazinyl]methyl}phenyl)propanoyl]-N-(4-fluorophenyl)-4-piperidinamine
- 1-[2-(4-{[(3R,5S)-3,5-dimethyl-1-piperazinyl]methyl}phenyl)propanoyl]-N-(3-fluorophenyl)-4-piperidinamine (E28)
- 1-[2-(4-{[(3R,5S)-3,5-dimethyl-1-piperazinyl]methyl}phenyl)-2-methylpropanoyl]-N-(4-fluorophenyl)-4-piperidinamine (E29)
- 1-[2-(4-{[(3R,5S)-3,5-dimethyl-1-piperazinyl]methyl}phenyl)-2-methylpropanoyl]-N-(3-fluorophenyl)-4-piperidinamine (E30)
- (3R,5S)-1-{[4-(2-{4-[(4-fluorophenyl)oxy]-1-piperidinyl}-1,1-dimethyl-2-oxoethyl)phenyl]methyl}-3,5-dimethylpiperazine (E31)
- N-(3-fluorophenyl)-1-[3-(5-{[(3S)-3-methyl-1-piperazinyl]methyl}-2-pyridinyl)propanoyl]-4-piperidinamine (E32)
- 1-[(3-Chloro-4-{[(3S)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-N-(3-fluorophenyl)-4-piperidinamine (E33)
- N-(2-fluorophenyl)-1-[(4-{[(3R)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-4-piperidinamine
- N-(3-fluorophenyl)-1-[(5-{[(3S)-3-methyl-1-piperazinyl]methyl}-2-pyridinyl)acetyl]-4-piperidinamine
- 2-({1-[(4-{[(3R)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-4-piperidinyl}amino)benzonitrile
- 2-fluoro-4-({1-[(4-{[(3S)-3-methyl-1-piperazinyl]methyl}phenyl)acetyl]-4-piperidinyl}amino)benzonitrile hydrochloride
wherein A is phenyl and X is CH2 or a pharmaceutically acceptable salt or solvate thereof, which process comprises reacting of a compound of formula (II)
wherein R1 and R2 are as defined in formula (I) and Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ), with a compound of formula (III)
wherein Y and R3 are as defined in formula (I), using reaction conditions suitable for a reductive alkylation, for example in the presence of a reducing agent such as sodium tri(acetoxy)borohydride in a suitable solvent such as dichloromethane or 1,2-dichloroethane.
-
- 1. Converting one compound of formula (I) into another compound of formula (I);
- 2. Removing any protecting group;
- 3. Forming a suitable pharmaceutical acceptable salt or solvate of the compound so formed.
in the presence of a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexylcarbodiimide (DCC), in a suitable solvent such as dichloromethane, dimethylformamide or mixtures thereof.
wherein R1 and R2 are as defined in formula (I) and Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ), with a compound of formula (IV) in the presence of a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexylcarbodiimide (DCC), in a suitable solvent such as dichloromethane, dimethylformamide or mixtures thereof.
- 1. Converting one compound of formula (I) into another compound of formula (I);
- 2. Removing any protecting group;
- 3. Forming a suitable pharmaceutical acceptable salt or solvate of the compound so formed.
- 1. Converting one compound of formula (I) into another compound of formula (I);
- 2. Removing any protecting group;
- 3. Forming a suitable pharmaceutical acceptable salt or solvate of the compound so formed.
wherein R1 and R2 are as defined in formula (I), Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ) and P is a suitable alkyl group such as methyl or ethyl, using aqueous sodium hydroxide in a suitable solvent such as 1,4-dioxane followed by acidification and decarboxylation by heating in a suitable solvent such as toluene.
wherein R1 and R2 are as defined in formula (I), L is a suitable leaving group such as a halogen, for example bromine, and Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ), with a suitable dialkyl malonate such as diethyl malonate under palladium catalysis in a suitable solvent such as 1,4-dioxane at reflux using a method similar to that described in S. L. Buchwald et al, J. Am. Chem. Soc., 2000, vol 122, p 1360-1370
wherein L is halogen, with a compound of formula (II), using reaction conditions suitable for a reductive amination, for example in the presence of a reducing agent such as sodium tri(acetoxy)borohydride in a suitable solvent such as dichloromethane or 1,2-dichloroethane.
wherein R1 and R2 are as defined in formula (I), Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ), and P is a suitable alkyl group such as methyl, using a suitable base such as aqueous sodium hydroxide in a suitable solvent such as tetrahydrofuran or 1,4-dioxane.
wherein P is a suitable alkyl group such as methyl and L is a suitable leaving group such as a halogen, for example bromine, in the presence of a suitable base such as diisopropylethylamine in a suitable solvent such as dimethylformamide.
wherein L is a halogen such as bromine, with methanol in the presence of trimethylsilyl chloride. Compounds of formula (XII) are commercially available.
wherein R1 and R2 are as defined in formula (I), Z is C(1-4)alkoxy and Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ) with a compound of formula (IV) in the presence of a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N-dicyclohexyl carbodiimide (DCC), in a suitable solvent such as dichloromethane, dimethylformamide or mixtures thereof.
- 1. Converting one compound of formula (I) into another compound of formula (I);
- 2. Removing any protecting group;
- 3. Forming a suitable pharmaceutical acceptable salt or solvate of the compound so formed.
- 1. Converting one compound of formula (I) into another compound of formula (I);
- 2. Removing any protecting group;
- 3. Forming a suitable pharmaceutical acceptable salt or solvate of the compound so formed.
wherein R1 and R2 are as defined in formula (I), Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ), Z is C(1-4)alkoxy and P is a suitable alkyl group such as methyl or ethyl, using aqueous sodium hydroxide followed by acidification and decarboxylation by heating in a suitable solvent such as tetrahydrofuran or 1,4-dioxane.
wherein Z is C(1-4)alkoxy and P is a suitable alkyl group such as methyl or ethyl, with a compound of formula (II) using reaction conditions suitable for a reductive amination, for example in the presence of a reducing agent such as sodium tri(acetoxy)borohydride in a suitable solvent such as dichloromethane or 1,2-dichloroethane.
wherein Z is C(1-4)alkoxy and P is alkyl such as ethyl, using a suitable aqueous acid, such as dilute hydrochloric acid, in a suitable solvent such as tetrahydrofuran.
wherein L is halogen such as bromine and Z is C(1-4)alkoxy, with a suitable dialkyl malonate such as diethyl malonate under palladium catalysis in a suitable solvent such as 1,4-dioxane at reflux using a method similar to that described in S. L. Buchwald et al, J. Am. Chem. Soc., 2000, vol 122, p 1360-1370.
wherein R1 and R2 are as defined in formula (I) and Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ) with a compound of formula (IV) in the presence of a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexylcarbodiimide (DCC), in a suitable solvent such as dichloromethane, dimethylformamide or mixtures thereof.
- 1. Converting one compound of formula (I) into another compound of formula (I);
- 2. Removing any protecting group;
- 3. Forming a suitable pharmaceutical acceptable salt or solvate of the compound so formed.
- 1. Converting one compound of formula (I) into another compound of formula (I);
- 2. Removing any protecting group;
- 3. Forming a suitable pharmaceutical acceptable salt or solvate of the compound so formed.
wherein R1 and R2 are as defined in formula (I), Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ), and P is a suitable alkyl group such as methyl, using a suitable base such as aqueous lithium hydroxide in a suitable solvent such as 1,4-dioxane.
wherein P is a suitable alkyl group such as methyl using a procedure similar to that described in J. F. Hartwig et al, J. Am. Chem. Soc., 2002, vol 124, p 12557-12565. The reaction may be carried out in the presence of a suitable base such as lithium di(cyclohexyl)amide, a suitable catalyst system such as bis(dibenzylidene) palladium (0)/tri(tert-butyl)phosphine and in a suitable solvent such as toluene.
wherein R1 and R2 are as defined in formula (I) and Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ) with a compound of formula (IV) in the presence of a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexylcarbodiimide (DCC), in a suitable solvent such as dichloromethane, dimethylformamide or mixtures thereof.
- 1. Converting one compound of formula (I) into another compound of formula (I);
- 2. Removing any protecting group;
- 3. Forming a suitable pharmaceutical acceptable salt or solvate of the compound so formed.
- 1. Converting one compound of formula (I) into another compound of formula (I);
- 2. Removing any protecting group;
- 3. Forming a suitable pharmaceutical acceptable salt or solvate of the compound so formed.
wherein R1 and R2 are as defined in formula (I), Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ) and P is a suitable alkyl group such as methyl or ethyl, using aqueous sodium hydroxide followed by acidification and decarboxylation by heating in a suitable solvent such as 1,4-dioxane or tetrahydrofuran.
wherein R1 and R2 are as defined in formula (I), Q is hydrogen or a suitable nitrogen protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ) and P is a suitable alkyl group such as methyl or ethyl, using standard alkylation conditions. For example reaction with a suitable base such as sodium hydride together with a suitable methylating agent such as iodomethane, in a suitable solvent, for example dimethylformamide.
wherein Y and R3 are as defined in formula (I), with a compound of formula (II) using reaction conditions suitable for a reductive amination, for example in the presence of a reducing agent such as sodium tri(acetoxy)borohydride in a suitable solvent such as dichloromethane or 1,2-dichloroethane.
- 1. Converting one compound of formula (I) into another compound of formula (I);
- 2. Removing any protecting group;
- 3. Forming a suitable pharmaceutical acceptable salt or solvate of the compound so formed.
with a compound of formula (IV) in the presence of a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexylcarbodiimide (DCC), in a suitable solvent such as dichloromethane, dimethylformamide or mixtures thereof.
wherein R1 and R2 are as defined in formula (I) and Q is a suitable protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ) in the presence of a suitable catalyst such as palladium black and in a suitable solvent such as methanol.
- 1. Converting one compound of formula (I) into another compound of formula (I);
- 2. Removing any protecting group;
- 3. Forming a suitable pharmaceutical acceptable salt or solvate of the compound so formed.
wherein R1 and R2 are as defined in formula (I) and Q is a suitable protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ), with a compound of formula (IV) in the presence of a suitable coupling reagent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) or N,N′-dicyclohexylcarbodiimide (DCC), in a suitable solvent such as dichloromethane, dimethylformamide or mixtures thereof.
wherein R1 and R2 are as defined in formula (I), Q is a suitable protecting group such as tert-butyloxycarbonyl (BOC) or benzyloxycarbonyl (CBZ), and P is a suitable alkyl group such as methyl, using a suitable base such as aqueous lithium hydroxide in a suitable solvent such as 1,4-dioxane.
wherein P is a suitable alkyl group such as methyl, with a compound of formula (II) using reaction conditions suitable for a reductive amination, for example in the presence of a reducing agent such as sodium tri(acetoxy)borohydride in a suitable solvent such as dichloromethane or 1,2-dichloroethane.
with a suitable alkyl acrylate such as methyl acrylate at elevated temperature, for example under microwave conditions, in the presence of a suitable catalyst system such as allyl palladium (II) chloride dimer/tri(o-tolyl)phosphine, and a suitable base, such as sodium acetate. A suitable solvent is dimethylformamide.
- Agilent 1100 Gradient Pump
- Agilent 1100 Autosampler
- Agilent 1100 DAD Dectector
- Agilent 1100 Degasser
- Agilent 1100 Oven
- Agilent 1100 Controller
- Waters ZQ Mass Spectrometer
- Sedere Sedex 55, Sedere Sedex 85 or Polymer Labs PL-ELS-2100
Software - Waters MassLynx version 4.0 SP2
Column
- A: Aqueous solvent=Water+0.05% Formic Acid
- B: Organic solvent=Acetonitrile+0.05% Formic Acid
Method
Time/min | % B | ||
0 | 3 | ||
0.1 | 3 | ||
4 | 97 | ||
4.8 | 97 | ||
4.9 | 3 | ||
5.0 | 3 | ||
Flow Rate
- 1 Waters 600 Gradient pump
- 1 Waters 2767 inject/collector
- 1 Waters Reagent manager
- 1 MicroMass ZQ Mass Spectrometer
- 1 Gilson Aspec—waste collector
- 1 Gilson 115 post-fraction UV detector
- 1 Computer System.
Software - MicroMass MassLynx v4.0
Column
- A: Aqueous solvent=Water+0.1% Formic Acid
- B: Organic solvent=MeCN:Water 95:5+0.05% Formic Acid
- Make up solvent=MeOH:Water 80:20+50 mMol Ammonium Acetate
- Needle rinse solvent=MeOH:Water:DMSO 80:10:10
Methods
- MDP 1.5-2.2=0-30% B
- MDP 2.0-2.8=5-30% B
- MDP 2.5-3.0=15-55% B
- MDP 2.8-4.0=30-80% B
- MDP 3.8-5.5=50-90% B
Flow Rate
- Bruker 400 MHz Ultrashield
- Bruker B-ACS60 Autosampler
- Bruker Advance 400 Console
- Bruker DPX250
- Bruker AVANCE 500
- Bruker DRX600
Software - User interface—NMR Kiosk
- Controlling software—XWin NMR version 3.0
Chromatography
- HCl—hydrochloric acid, hydrogen chloride
- NaHCO3—sodium hydrogen carbonate
- Na2SO—sodium sulfate
- 1,2-DCE—1,2-dichloroethane,
- NaOH—sodium hydroxide
- DCM—dichloromethane
- DMF—N,N-dimethylformamide
- THF—tetrahydrofuran
- MeOH—methanol,
- EtOAc—ethyl acetate
- MgSO4—magnesium sulfate
- NH3-ammonia
- TFA—trifluoroacetic acid
- Et2O—diethyl ether
- CDCl3-deuterochloroform
- DCC—N,N′-dicyclohexylcarbodiimide
- BINAP—(±)-2,2′-bis(diphenylphosphino)-1,1′-binaphthalene
Ex- | Amine | |||
ample | Precursor | Compound | YR3 | MH+ |
3 | D2 | N-(4-Fluorophenyl)-1-[(4-{[(3S)-3- methyl-1-piperazinyl]methyl}- phenyl)acetyl]-4-piperidinamine (E3) |
|
425 |
4 | D10b | 3-({1-[(4-{[(3S)-3-Methyl-1- piperazinyl]methyl}phenyl)acetyl]- 4-piperidinyl}amino)benzonitrile (E4) |
|
432 |
5 | D11b | 4-({1-[(4-{[(3S)-3-Methyl-1- piperazinyl]methyl}phenyl)acetyl]- 4-piperidinyl}amino)benzonitrile (E5) |
|
432 |
6 | D9b | N-(3,4-Difluorophenyl)-1-[(4-{[(3S)- 3-methyl-1-piperazinyl]methyl}- phenyl)acetyl]-4-piperidinamine (E6) |
|
443 |
7 | D12b | N-[4-Fluoro-3-(methyloxy)phenyl]- 1-[(4-{[(3S)-3-methyl-1- piperazinyl]methyl}phenyl)acetyl]- 4-piperidinamine (E7) |
|
455 |
8 | D15 | (3S)-1-{[4-(2-{4-[(4- Fluorophenyl)oxy]-1-piperidinyl}- 2-oxoethyl)phenyl]methyl}-3- methylpiperazine (E8) |
|
426 |
9 | D14 | (3S)-1-{[4-(2-{4-[(3- Fluorophenyl)oxy]-1-piperidinyl}- 2-oxoethyl)phenyl]methyl}-3- methylpiperazine (E9) |
|
426 |
10 | D21 | 1-[(4-{[(3S)-3-Methyl-1- piperazinyl]methyl}phenyl)acetyl]- N-[3-(trifluoromethyl)phenyl]-4- piperidinamine (E10) |
|
475 |
11 | D23 | 1-[(4-{[(3S)-3-Methyl-1 - piperazinyl]methyl}phenyl)acetyl]- N-[4-(trifluoromethyl)phenyl]-4- piperidinamine (E11) |
|
475 |
Amine | ||||
Example | Precursor | Compound | YR3 | MH+ |
12 | D5B | N-(3-Fluorophenyl)-1-{[4-(1- piperazinylmethyl)phenyl]acetyl}- 4-piperidinamine (E12) |
|
411 |
Amine | ||||
Example | Precursor | Compound | YR3 | MH+ |
14 | D9b | N-(3,4-Difluorophenyl)-1-[(4- {[(3R)-3-methyl-1- piperazinyl]methyl}phenyl)acetyl]- 4-piperidinamine (E14) |
|
443 |
15 | D15 | (3R)-1-{[4-(2-{4-[(4- Fluorophenyl)oxy]-1-piperidinyl}- 2-oxoethyl)phenyl]methyl}-3- methylpiperazine (E15) |
|
426 |
16 | D14 | (3R)-1-{[4-(2-{4-[(3- Fluorophenyl)oxy]-1-piperidinyl}- 2-oxoethyl)phenyl]methyl}-3- methylpiperazine (E16) |
|
426 |
17 | D31 | 4-({1-[(4-{[(3R)-3-Methyl-1- piperazinyl]methyl}phenyl)acetyl]- 4-piperidinyl}oxy)benzonitrile (E17) |
|
433 |
18 | D11b | 4-({1-[(4-{[(3R)-3-Methyl-1- piperazinyl]methyl}phenyl)acetyl]- 4-piperidinyl}amino)benzonitrile (E18) |
|
432 |
19 | D10b | 3-({1-[(4-{[(3R)-3-Methyl-1- piperazinyl]methyl}phenyl)acetyl]- 4-piperidinyl}amino)benzonitrile (E19) |
|
432 |
20 | D21 | 1-[(4-{[(3R)-3-Methyl-1- piperazinyl]methyl}phenyl)acetyl]- N-[3-(trifiuoromethyl)phenyl]-4- piperidinamine (E20) |
|
475 |
Example | Compound | YR3 | MH+ |
24 | 1-[3-(4-{[(3R,5S)-3,5-Dimethyl-1- piperazinyl]methyl}phenyl)propanoyl]- N-(3-fluorophenyl)-4-piperidinamine (E24) |
|
453 |
Example | Compound | YR3 | MH+ |
26 | N-(3-Fluorophenyl)-1-[3-(4-{[(3S)- 3-methyl-1- piperazinyl]methyl}phenyl) propanoyl]-4-piperidinamine (E26) |
|
439 |
Example | Compound | YR3 | MH+ |
28 | 1-[2-(4-{[(3R,5S)-3,5-Dimethyl-1- piperazinyl]methyl}phenyl)propanoyl]- N-(3-fluorophenyl)-4-piperidinamine (E28) |
|
453 |
Amine | ||||
Example | Precursor | Compound | YR3 | MH+ |
30 | D5b | 1-[2-(4-{[(3R,5S)-3,5-Dimethyl-1- piperazinyl]methyl}phenyl)-2- methylpropanoyl]-N-(3- fluorophenyl)-4-piperidinamine (E30) |
|
467 |
31 | D15 | (3R,5S)-1-{[4-(2-{4-[(4- Fluorophenyl)oxy]-1-piperidinyl}- 1,1-dimethyl-2- oxoethyl)phenyl]methyl}-3,5- dimethylpiperazine (E31) |
|
468 |
Claims (16)
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GB0515381A GB0515381D0 (en) | 2005-07-26 | 2005-07-26 | Compounds |
GB0515381.2 | 2005-07-26 | ||
GB0611469.8 | 2006-06-09 | ||
GB0611469A GB0611469D0 (en) | 2006-06-09 | 2006-06-09 | Compounds |
PCT/EP2006/007390 WO2007012479A2 (en) | 2005-07-26 | 2006-07-24 | Benzylpiperazine derivates and their medical use |
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US20090054456A1 US20090054456A1 (en) | 2009-02-26 |
US8536182B2 true US8536182B2 (en) | 2013-09-17 |
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MY150098A (en) * | 2005-07-26 | 2013-11-29 | Glaxo Group Ltd | Benzylpiperazine derivates and their medical use |
GB0524814D0 (en) * | 2005-12-05 | 2006-01-11 | Glaxo Group Ltd | Compounds |
CA2633568A1 (en) | 2006-01-27 | 2007-08-09 | M's Science Corporation | Piperidine and piperazine derivatives |
MX2009000110A (en) | 2006-06-28 | 2009-01-23 | Glaxo Group Ltd | Piperazinyl derivatives useful in the treatment of gpr38 receptor mediated diseases. |
GB0723317D0 (en) | 2007-11-28 | 2008-01-09 | Glaxo Group Ltd | Compounds |
KR101575703B1 (en) | 2009-02-27 | 2015-12-10 | 라퀄리아 파마 인코포레이티드 | Oxyindole derivatives with motilin receptor agonistic activity |
WO2011092293A2 (en) | 2010-02-01 | 2011-08-04 | Novartis Ag | Cyclohexyl amide derivatives as crf receptor antagonists |
JP2013518085A (en) | 2010-02-01 | 2013-05-20 | ノバルティス アーゲー | Pyrazolo [5,1b] oxazole derivatives as CRF-1 receptor antagonists |
JP5748777B2 (en) | 2010-02-02 | 2015-07-15 | ノバルティス アーゲー | Cyclohexylamide derivatives as CRF receptor antagonists |
CN113292485B (en) * | 2021-06-08 | 2023-10-27 | 河南大学 | Benzyl piperazine urea TRPV1 antagonizing and MOR agonizing double-target medicine and its prepn and application |
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